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Article

Evidence of H3 K27M mutations in posterior fossa ependymomas.

Acta neuropathologica - 1 Oct 2016

Gessi Marco, Capper David, Sahm Felix, Huang Kristin, von Deimling Andreas, Tippelt Stephan, Fleischhack Gudrun, Scherbaum Daniel, Alfer Joachim, Juhnke Björn-Ole, von Hoff Katja, Rutkowski Stefan, Warmuth-Metz Monika, Chavez Lukas, Pfister Stefan M, Pietsch Torsten, Jones David T W, Sturm Dominik

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PMID: 27539613
DOI: 10.1007/s00401-016-1608-3

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Evidence of H3 K27M mutations in posterior fossa ependymomas.PMID 27539613Read ↗

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Detection of H3K27M mutation in cases of brain stem subependymomaSemantic proximity Read ↗

Posterior fossa ependymoma H3 K27-mutant: an integrated radiological and histomolecular tumor analysisSemantic proximity Read ↗

Molecular heterogeneity and CXorf67 alterations in posterior fossa group A (PFA) ependymomas.Semantic proximity Read ↗

Evidence for BRAF V600E and H3F3A K27M double mutations in paediatric glial and glioneuronal tumours.Semantic proximity Read ↗

EZH2 inhibitory protein (EZHIP/Cxorf67) expression correlates strongly with H3K27me3 loss in posterior fossa ependymomas and is mutually exclusive with H3K27M mutations.Semantic proximity Read ↗

Lowered H3K27me3 and DNA hypomethylation define poorly prognostic pediatric posterior fossa ependymomas.Semantic proximity Read ↗

Mutation profiling of anaplastic ependymoma grade III by Ion Proton next generation DNA sequencingSemantic proximity Read ↗

Recurrent ACVR1 mutations in posterior fossa ependymoma.Semantic proximity Read ↗

FGFR1 N546K and H3F3A K27M mutations in a diffuse leptomeningeal tumour with glial and neuronal markers.Semantic proximity Read ↗

Recurrent posterior fossa group A (PFA) ependymoma in a young child with constitutional mismatch repair deficiency (CMMRD).Semantic proximity Read ↗

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